NDC Code(s) : 55700-266-60
Packager : Lake Erie Medical DBA Quality Care Products LLC

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

Senokot-Sstandardized senna concentrate and docusate sodium TABLET
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:55700-266(NDC:67618-310)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SENNOSIDES(UNII: 3FYP5M0IJX)
(SENNOSIDES - UNII:3FYP5M0IJX) 		SENNOSIDES8.6 mg
DOCUSATE SODIUM(UNII: F05Q2T2JA0)
(DOCUSATE - UNII:M7P27195AG) 		DOCUSATE SODIUM50 mg
Inactive Ingredients
Ingredient Name Strength
CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS(UNII: L11K75P92J)
D&C YELLOW NO. 10(UNII: 35SW5USQ3G)
FD&C YELLOW NO. 6(UNII: H77VEI93A8)
EGG PHOSPHOLIPIDS(UNII: 1Z74184RGV)
MAGNESIUM STEARATE(UNII: 70097M6I30)
CELLULOSE, MICROCRYSTALLINE(UNII: OP1R32D61U)
POLYETHYLENE GLYCOLS(UNII: 3WJQ0SDW1A)
POLYVINYL ALCOHOL(UNII: 532B59J990)
STARCH, CORN(UNII: O8232NY3SJ)
SODIUM BENZOATE(UNII: OJ245FE5EU)
TALC(UNII: 7SEV7J4R1U)
TITANIUM DIOXIDE(UNII: 15FIX9V2JP)
Product Characteristics
Color ORANGE Score no score
Shape ROUND Size 10 mm
Flavor Imprint Code P
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:55700-266-601 in 1 CARTON
160 in 1 BOTTLE, PLASTIC Type 0: Not a Combination Product
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part334 10/01/1974

PRINCIPAL DISPLAY PANEL

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